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Clinical Laboratory Director & Vice President, Translational & Computational Pathology LOCATION: North Brunswick, New Jersey JOB TYPE: Full-Time SCHEDULE: • Monday - Friday, • Standard Day Shift, • No On-Call Responsibilities, • No Weekend Requirements SETTING: • On-Site, • Biotechnology & Oncology Diagnostics, • Clinical Laboratory Environment, • Translational Research & Companion Diagnostics, • Digital & Computational Pathology IMPORTANT DETAILS: • Executive leadership role with Clinical Laboratory Director responsibilities, • Opportunity to lead pathology, biomarker, and companion diagnostic programs, • Focus on translational oncology, digital pathology, and AI-enabled diagnostics, • Collaborate with pathology, AI/ML, engineering, and research teams, • Ideal for candidates who enjoy both strategic leadership and hands-on scientific involvement SUMMARY: We are seeking an accomplished physician-scientist and executive leader to serve as Clinical Laboratory Director & Vice President, Translational & Computational Pathology. This role combines laboratory leadership, regulatory oversight, translational research, companion diagnostics, and computational pathology initiatives. The successful candidate will drive innovation in oncology diagnostics while leading laboratory operations and contributing to scientific strategy, product development, and industry partnerships. ROLES & RESPONSIBILITIES: Clinical Laboratory Leadership • Serve as the designated Clinical Laboratory Director under applicable regulatory standards, • Maintain oversight of laboratory quality systems, accreditation, inspections, and audits, • Lead pathology operations, histology workflows, tissue processing, and diagnostic testing, • Establish laboratory policies, procedures, and quality standards, • Ensure continuous regulatory compliance and operational excellence Translational Pathology & Companion Diagnostics • Lead pathology strategy supporting biomarker discovery and translational research, • Oversee development, validation, and implementation of pathology-based assays, • Collaborate with pharmaceutical partners on companion diagnostic and biomarker programs, • Support oncology-focused translational research initiatives, • Expand pathology and companion diagnostic capabilities Digital & Computational Pathology • Lead digital pathology and computational pathology initiatives, • Collaborate with AI/ML, engineering, and data science teams, • Support whole-slide imaging, image analysis, and quantitative tissue analysis platforms, • Establish standards for AI-enabled pathology applications Executive Leadership • Provide scientific leadership across pathology and diagnostic programs, • Build relationships with industry partners, pharmaceutical organizations, and academic institutions, • Support publications, presentations, and scientific communications, • Drive cross-functional collaboration across research and development teams QUALIFICATIONS: Required • MD or DO from an accredited institution, • Board Certification in Anatomic Pathology and Clinical Pathology (AP/CP), • Eligible to serve as a Clinical Laboratory Director under CLIA regulations, • Active unrestricted medical license or ability to obtain state licensure, • Minimum 5 years of leadership experience within a pathology laboratory, diagnostics company, pharmaceutical organization, academic medical center, or CRO, • Experience in pathology assay development, validation, and laboratory operations, • Experience supporting clinical trials, translational medicine, companion diagnostics, or pharmaceutical-sponsored research Preferred • Translational oncology and biomarker development experience, • Companion Diagnostics (CDx) experience, • Immunohistochemistry (IHC) assay development and validation expertise, • Digital pathology implementation experience, • Strong scientific publication and presentation record Highly Desired • Computational pathology experience, • AI-assisted pathology workflows, • Whole-slide imaging (WSI) implementation, • Spatial biology and multiplex tissue analysis, • Experience bringing diagnostic products or companion diagnostics to market BENEFITS: • Medical Insurance, • Dental Insurance, • Vision Insurance, • 401(k) Retirement Plan, • Generous Paid Time Off, • Professional Development Support, • Continuing Education Resources, • Relocation Assistance Available

Job DescriptionSalary: Princeton NuEnergy (PNE) is excited to announce future opportunities to join our innovative Research & Development team, focused on pioneering advancements in the direct recycling and upcycling of spent Lithium-ion battery materials. Our mission is to deliver a cost-efficient, environmentally friendly solution to the current industry pain points of high operational costs and low efficiency in battery recycling. We aim to solve these challenges by improving battery recycling efficiency and purity, thereby revolutionizing the lithium-ion battery recycling landscape. About Us: PNE is a lithium-ion battery direct recycling and critical materials recovery innovator, founded out of Princeton University. At its core, PNE's patented recycling technology is based on a low-temperature plasma-assisted separation process (LPAS) that does not damage but, rather, reclaims and repairs cathode material from spent lithium-ion batteries and manufacturing scrap at half the cost with significantly lower waste when compared with existing traditional recycling processes. Our state-of-the-art laboratory is located in Princeton, New Jersey, where we are dedicated to pushing the boundaries of sustainable energy technologies. We are building a team of passionate and talented individuals to drive forward our cutting-edge research initiatives. Potential Roles: We anticipate openings for the following positions in the near future: • Research Scientist, • Process Engineer, • Technician Ideal Candidates: We welcome applications from candidates with expertise in: • Battery cathode material synthesis and related research experience., • Plasma physics, particularly in device development and experimental applications., • Chemical Engineering (with a focus on inorganic chemistry), Materials Science & Engineering, Chemistry, or related areas of study. If you are passionate about sustainability, innovation, and advancing the future of energy storage, we would love to hear from you! Princeton NuEnergy, Inc. is proud to be an Equal Opportunity Employer All qualified applicants will receive consideration for employment without regard to race, color, gender, sexual orientation, gender identity or expression, religion, national origin, marital status, age, disability, veteran status, genetic information, or any other protected status under federal, state, and local laws.

Job DescriptionCompany Description Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organization services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organizations. It also has a rapidly developing presence in highly specialized and molecular clinical diagnostic testing and in-vitro diagnostic products. In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralized and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. 2025, Eurofins generated total revenues of EUR € 7.296 billion, and has been among the best performing stocks in Europe over the past 20 years. Job Description We are searching for an Entry Level Scientist to support our growing team. Scientist responsibilities include, but are not limited to, the following: • Set-up and conduct experiments in accordance with Protocol and SOP's., • Efficiently carry out procedures necessary to complete each project with minimal supervision., • Prepare test solutions and diets in accordance with directions., • dosing, necropsy and other procedures., • Dose, evaluate responses, perform necropsies, and collect blood, urine, fecal and tissue specimens in accordance with standard operating procedures and protocols., • Meticulously maintain precise records of all experiments in accordance with good laboratory practices., • Assist in writing of reports., • Follow all PSL safety requirements., • Ability to safely wear a respirator requiredQualifications The ideal candidate would possess: • Strong computer, scientific, and organizational skills, • Excellent communication (oral and written) and attention to detail, • Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude, • Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies Basic Minimum Qualifications: • Bachelor's degree in laboratory animal medicine, toxicology, animal science or biology is preferred, or equivalent directly-related experience (two years of directly related industry experience is equivalent to one full-time year of college in related major), • Authorization to work in the United States indefinitely without restriction or sponsorship Additional Information Position is full-time, Monday-Friday 8am-5pm. Candidates within a commutable distance of South Brunswick, NJ are encouraged to apply. Pay range is $21/h to $25/h depending on experience. Excellent full time benefits including: • Comprehensive medical coverage, dental, and vision options, • Life and disability insurance, • 401(k) with company match, • Paid vacation and holidays Eurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.

Job DescriptionAbout GenScriptGenScript Biotech Corporation (Stock Code: 1548.HK) is a global biotechnology group. Founded in 2002, GenScript has an established global presence across North America, Europe, the Greater China, and Asia Pacific. GenScript's businesses encompass four major categories based on its leading gene synthesis technology, including operation as a Life Science CRO, enzyme and synthetic biology products, biologics development and manufacturing, and cell therapy.GenScript is committed to striving towards its vision of being the most reliable biotech company in the world to make humans and nature healthier through biotechnology. Genscript is seeking a motivated and detail-oriented HTP Analytical QC Associate Scientist to join our dynamic US Protein Department in Piscataway, New Jersey. The estimated salary range is $60,000 - $75,000, depending on experience. Reporting to: Supervisor of HTP Platform Employment Type: Full-time Role Description: We are seeking a detail-oriented and proactive Associate Scientist to join our High-Throughput Protein Analytical QC Laboratory. This role is responsible for performing analytical characterization and quality control testing of recombinant proteins generated from high-throughput production workflows. The successful candidate will play a critical role in ensuring protein identity, purity, and overall quality through robust analytical methodologies. This position operates in a data-driven and quality-focused environment where accuracy, reproducibility, and data integrity are essential. The ideal candidate will have hands-on experience with protein analytical techniques and familiarity with laboratory data management systems such as ELN, LIMS, or equivalent platforms. Key Responsibilities: • Perform routine and non-routine analytical and QC testing to evaluate protein identity, purity, and quality attributes., • Execute a range of protein characterization assays, including:, • HPLC / UPLC (e.g., SEC, RP, IEX), • Capillary Electrophoresis (CE, iCE/cIEF), • SDS-PAGE, • Western blot, • LC-MS, • Endotoxin assays, • Prepare samples, reagents, buffers, and standards in accordance with established protocols and assay requirements., • Perform sample preparation workflows, including use of automated liquid handling systems where applicable., • Analyze, interpret, and document experimental data in ELN, LIMS, or equivalent systems, ensuring compliance with data integrity standards (e.g., ALCOA+ principles)., • Support method troubleshooting and optimization, ensuring assay robustness, reproducibility, and consistency across runs., • Maintain laboratory instruments and ensure proper calibration and performance, supporting compliance with quality and safety standards., • Collaborate with cross-functional teams (e.g., protein production, process development) to support project timelines and deliverables., • Contribute to continuous improvement initiatives, including method refinement, workflow efficiency, and data quality enhancement. Qualifications: • BS or MS in Biochemistry, Analytical Chemistry, Biotechnology, or a related field with 2+ years of relevant experience in protein analytical characterization or QC., • Hands-on experience with protein analytical techniques such as HPLC/UPLC, CE, SDS-PAGE, Western blot, LC-MS, or endotoxin assays., • Familiarity with protein characterization workflows, including purity, aggregation, and identity analysis., • Experience with laboratory data systems (ELN, LIMS, or similar) and strong documentation practices., • Strong attention to detail and commitment to data integrity, accuracy, and reproducibility., • Experience in a CRO/CDMO or regulated QC environment is preferred. #LI-EB1 #GS GenScript USA Inc/ProBio Inc. is a proud equal opportunity/affirmative action employer committed to attracting, retaining, and maximizing the performance of a diverse and inclusive workforce. It is the Company's policy to ensure equal employment opportunity without discrimination or harassment based on race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity or expression, age, disability, national origin, marital or domestic/civil partnership status, genetic information, citizenship status, uniformed service member or veteran status, or any other characteristic protected by law. GenScript USA Inc./ProBio Inc. maintains a drug-free workplace. Please note: Genscript USA Inc./ProBio Inc. will only contact candidates through verified application sources. GenScript/Probio does not request personal information from candidates through individual email or any other platform.

Job Description Clinical Laboratory Director & Vice President, Translational & Computational Pathology LOCATION: North Brunswick, New Jersey JOB TYPE: Full-Time SCHEDULE: • Monday - Friday, • Standard Day Shift, • No On-Call Responsibilities, • No Weekend Requirements SETTING: • On-Site, • Biotechnology & Oncology Diagnostics, • Clinical Laboratory Environment, • Translational Research & Companion Diagnostics, • Digital & Computational Pathology IMPORTANT DETAILS: • Executive leadership role with Clinical Laboratory Director responsibilities, • Opportunity to lead pathology, biomarker, and companion diagnostic programs, • Focus on translational oncology, digital pathology, and AI-enabled diagnostics, • Collaborate with pathology, AI/ML, engineering, and research teams, • Ideal for candidates who enjoy both strategic leadership and hands-on scientific involvement SUMMARY: We are seeking an accomplished physician-scientist and executive leader to serve as Clinical Laboratory Director & Vice President, Translational & Computational Pathology. This role combines laboratory leadership, regulatory oversight, translational research, companion diagnostics, and computational pathology initiatives. The successful candidate will drive innovation in oncology diagnostics while leading laboratory operations and contributing to scientific strategy, product development, and industry partnerships. ROLES & RESPONSIBILITIES: Clinical Laboratory Leadership • Serve as the designated Clinical Laboratory Director under applicable regulatory standards, • Maintain oversight of laboratory quality systems, accreditation, inspections, and audits, • Lead pathology operations, histology workflows, tissue processing, and diagnostic testing, • Establish laboratory policies, procedures, and quality standards, • Ensure continuous regulatory compliance and operational excellence Translational Pathology & Companion Diagnostics • Lead pathology strategy supporting biomarker discovery and translational research, • Oversee development, validation, and implementation of pathology-based assays, • Collaborate with pharmaceutical partners on companion diagnostic and biomarker programs, • Support oncology-focused translational research initiatives, • Expand pathology and companion diagnostic capabilities Digital & Computational Pathology • Lead digital pathology and computational pathology initiatives, • Collaborate with AI/ML, engineering, and data science teams, • Support whole-slide imaging, image analysis, and quantitative tissue analysis platforms, • Establish standards for AI-enabled pathology applications Executive Leadership • Provide scientific leadership across pathology and diagnostic programs, • Build relationships with industry partners, pharmaceutical organizations, and academic institutions, • Support publications, presentations, and scientific communications, • Drive cross-functional collaboration across research and development teams QUALIFICATIONS: Required • MD or DO from an accredited institution, • Board Certification in Anatomic Pathology and Clinical Pathology (AP/CP), • Eligible to serve as a Clinical Laboratory Director under CLIA regulations, • Active unrestricted medical license or ability to obtain state licensure, • Minimum 5 years of leadership experience within a pathology laboratory, diagnostics company, pharmaceutical organization, academic medical center, or CRO, • Experience in pathology assay development, validation, and laboratory operations, • Experience supporting clinical trials, translational medicine, companion diagnostics, or pharmaceutical-sponsored research Preferred • Translational oncology and biomarker development experience, • Companion Diagnostics (CDx) experience, • Immunohistochemistry (IHC) assay development and validation expertise, • Digital pathology implementation experience, • Strong scientific publication and presentation record Highly Desired • Computational pathology experience, • AI-assisted pathology workflows, • Whole-slide imaging (WSI) implementation, • Spatial biology and multiplex tissue analysis, • Experience bringing diagnostic products or companion diagnostics to market BENEFITS: • Medical Insurance, • Dental Insurance, • Vision Insurance, • 401(k) Retirement Plan, • Generous Paid Time Off, • Professional Development Support, • Continuing Education Resources, • Relocation Assistance Available Company DescriptionProtouch Staffing is a trusted staffing partner specializing in connecting skilled professionals with top employers. While we originally focused on healthcare staffing, we’ve expanded into legal and other domains to meet evolving workforce needs across industries.Protouch Staffing is a trusted staffing partner specializing in connecting skilled professionals with top employers. While we originally focused on healthcare staffing, we’ve expanded into legal and other domains to meet evolving workforce needs across industries.

Job DescriptionJob Title: Scientist – Medical Device Toxicology (CRO) Job Description This role focuses on preparing and testing a wide range of medical devices within a contract research organization (CRO) environment to support in vivo toxicology studies and help advance treatments, including therapies for cancer. The scientist handles devices ranging from simple solid materials to complex implants, such as tubes, syringes, and various plastic components, and prepares extracts in accordance with ISO standards and Good Laboratory Practices (GLP). This position requires a hands-on leader who brings strong technical expertise in medical device extraction, supports and trains less experienced staff, and maintains meticulous documentation while working in a fast-paced, client-driven setting. Responsibilities • Receive, evaluate, and process medical device test articles submitted for testing., • Review incoming devices to determine appropriate tests and preparation procedures in accordance with ISO standards and internal protocols., • Confirm that all required instructions and documentation accompany each device and verify surface area measurements and related details., • Determine the surface area of each device or device component and calculate the required extraction ratio for testing., • Prepare extractions from medical devices, creating liquid extracts that will be dosed to animals in toxicology studies., • Handle a broad range of devices, such as syringes, tubing sets, and other components, including measuring and calculating surface areas for partial or fully submerged configurations while excluding non-relevant parts (for example, end caps that do not contact the patient)., • Prepare samples and dosing solutions using aseptic technique and in strict accordance with standard operating procedures and study protocols., • Coordinate and communicate sample preparation and scheduling with scientific staff and Study Directors to align with study timelines and changing client needs., • Run assays and execute scheduled laboratory activities as outlined in weekly study schedules and protocols., • Participate in dosing studies in the vivarium, including obtaining animal body weights and administering test materials via appropriate routes such as intravenous injection., • Monitor and observe animals following dosing, including wrapping or restraining animals when needed to ensure proper handling and safety., • Perform single-injection studies and related observations, documenting all procedures and outcomes accurately., • Meticulously maintain precise, complete, and accurate records of all preparations, dosing activities, and assay results in compliance with GLP requirements., • Perform basic mathematical calculations to support surface area determinations, extraction ratios, and dosing calculations., • Maintain a clean, organized, and well-documented work area to support efficient and compliant study execution., • Follow all laboratory and facility safety requirements, including the ability to safely wear a respirator when needed., • Lead and mentor less experienced personnel, providing training on device preparation, extraction techniques, documentation practices, and GLP expectations., • Adapt to a fast-paced, schedule-driven environment where priorities may shift based on client demands., • Support cage wash and cleaning activities related to animal studies as needed to maintain a compliant and sanitary environment., • Contribute to study reporting by providing accurate data, documentation, and assay results to scientific staff and Study Directors.Essential Skills, • Direct hands-on experience preparing extracts of medical devices in a contract research organization (CRO) environment., • Practical experience handling a variety of medical devices, from simple components to complex implants, for testing and extraction., • Working knowledge and application of ISO standards related to medical device testing and extraction., • Strong understanding and practice of Good Laboratory Practices (GLP), with the ability to maintain meticulous and accurate records., • Experience preparing dosing solutions and extractions that are administered to animals in toxicology studies., • Hands-on experience with toxicology-related procedures, including dosing and in vivo study support., • Ability to perform basic mathematical calculations, including surface area determinations and extraction ratio calculations., • Proven ability to follow detailed written and verbal instructions, standard operating procedures, and study protocols., • Demonstrated integrity, strong sense of responsibility, and commitment to ethical and compliant laboratory work., • Strong organizational skills with the ability to manage a broad spectrum of responsibilities in a fast-paced environment., • Capability to work independently while also collaborating effectively with scientific staff and Study Directors., • Ability to safely wear a respirator when required by specific tasks or safety protocols.Additional Skills & Qualifications, • Leadership experience in a laboratory or CRO setting, including mentoring and training less experienced staff., • Experience working directly with animals in a vivarium setting, including dosing, body weight collection, and observation., • Familiarity with intravenous (IV) dosing and related dosing techniques in animal studies., • Background in toxicology, pharmacology, or related life sciences disciplines., • Experience with medical device preparation for testing, including disassembly, extraction practices, and readiness for ISO-compliant testing., • Comfort working in a fast-paced environment with changing schedules driven by client needs., • Strong attention to detail in paperwork, documentation, and record-keeping to support GLP compliance., • Ability to communicate clearly and professionally with cross-functional scientific teams., • Motivation to contribute to research that supports the development of therapies, including those aimed at curing cancer.Work Environment The role is based within a contract research organization (CRO) that conducts animal studies and medical device testing in a vivarium and laboratory setting. The environment is fast-paced and schedule-driven, with priorities that may shift based on client timelines and study requirements. You will work hands-on with medical devices, laboratory equipment, and animal dosing setups, following ISO standards, GLP, and strict safety protocols. The position involves close collaboration with scientific staff and Study Directors, as well as leadership and training responsibilities with less experienced team members. The work includes time in animal facilities, cage wash and cleaning support as needed, and adherence to all facility safety requirements, including the use of personal protective equipment and respirators when required. The culture emphasizes scientific rigor, integrity, meticulous documentation, and a shared commitment to advancing research that supports treatments for serious diseases, including cancer. Job Type & Location This is a Contract to Hire position based out of DAYTON, NJ. Pay and Benefits The pay range for this position is $30.00 - $35.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision, • Critical Illness, Accident, and Hospital, • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available, • Life Insurance (Voluntary Life & AD&D for the employee and dependents), • Short and long-term disability, • Health Spending Account (HSA), • Transportation benefits, • Employee Assistance Program, • Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in DAYTON,NJ. Application Deadline This position is anticipated to close on Jun 16, 2026. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options. San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records. Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability. Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.

Job DescriptionAbout GenScriptGenScript Biotech Corporation (Stock Code: 1548.HK) is a global biotechnology group. Founded in 2002, GenScript has an established global presence across North America, Europe, the Greater China, and Asia Pacific. GenScript's businesses encompass four major categories based on its leading gene synthesis technology, including operation as a Life Science CRO, enzyme and synthetic biology products, biologics development and manufacturing, and cell therapy.GenScript is committed to striving towards its vision of being the most reliable biotech company in the world to make humans and nature healthier through biotechnology. Genscript is seeking a motivated and detail-oriented HTP Production Associate Scientist to join our dynamic US Protein Department in Piscataway, New Jersey. The estimated salary range is $60,000 - $75,000, depending on experience. Reporting to: Supervisor of HTP Platform Employment Type: Full-time Role Description: We are seeking a detail-oriented and proactive Associate Scientist to join our High-Throughput Protein Production Laboratory. This role supports automation-driven workflows for recombinant protein generation using advanced liquid handling platforms. The successful candidate will contribute to large-scale, high-throughput protein production processes, including upstream handling, purification, and downstream analytical characterization. This position operates in a highly process-driven environment where automation, aseptic technique, and robust sample tracking are critical. The ideal candidate is comfortable working with automated laboratory systems, possesses strong organizational skills, and has experience with laboratory data management platforms such as ELN, LIMS, or similar systems. Key Responsibilities: • Execute high-throughput protein production workflows using automated liquid handling systems (e.g., Lynx platform) in a reproducible and efficient manner., • Operate and monitor automated protocols for processes including:, • Mammalian cell culture handling, • Protein purification workflows, • Sample aliquoting and distribution, • Perform laboratory operations under aseptic conditions to support recombinant protein expression and processing activities., • Monitor automated runs and identify workflow deviations, ensuring adherence to established SOPs and quality standards., • Manage high-throughput sample workflows, including sample tracking, plate mapping, labeling, and inventory control to ensure traceability and data integrity., • Document experimental procedures and process parameters accurately in ELN, LIMS, or equivalent systems in compliance with data integrity requirements., • Support maintenance, calibration, and troubleshooting of automation platforms and associated laboratory equipment., • Collaborate with cross-functional teams (analytical, process development, and operations) to meet project timelines and deliverables., • Contribute to continuous improvement initiatives, including workflow optimization, automation efficiency, and process scalability. Qualifications: • BS or MS in Biochemistry, Biotechnology, Analytical Chemistry, or a related field with 2+ years of relevant laboratory experience in protein production or characterization., • Hands-on experience with automated liquid handling systems (e.g., Dynamic Devices Lynx, Hamilton, Tecan) is strongly preferred., • Familiarity with protein production workflows, including mammalian cell culture, purification, or high-throughput screening environments., • Experience with laboratory data systems such as ELN, LIMS, or similar platforms., • Strong attention to detail, organizational skills, and commitment to data integrity and traceability., • Experience in a CRO/CDMO or high-throughput platform environment is a plus. #LI-EB1 #GS GenScript USA Inc/ProBio Inc. is a proud equal opportunity/affirmative action employer committed to attracting, retaining, and maximizing the performance of a diverse and inclusive workforce. It is the Company's policy to ensure equal employment opportunity without discrimination or harassment based on race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity or expression, age, disability, national origin, marital or domestic/civil partnership status, genetic information, citizenship status, uniformed service member or veteran status, or any other characteristic protected by law. GenScript USA Inc./ProBio Inc. maintains a drug-free workplace. Please note: Genscript USA Inc./ProBio Inc. will only contact candidates through verified application sources. GenScript/Probio does not request personal information from candidates through individual email or any other platform.

Job DescriptionJob Title: Assay Development Scientist (POC IVD Consultant / Contractor) Job Description This consulting role supports a fast-growing medical device organization that develops innovative point-of-care diagnostic platforms for decentralized clinical testing. The Assay Development Scientist will lead the design, optimization, and productization of clinical chemistry assays for a Lab-on-Spin-Disk / centrifugal microfluidic diagnostic platform, translating assays from feasibility to robust, manufacturable in vitro diagnostic products. The position focuses on dry and stabilized reagent formats, including lyophilized reagent beads, and involves close collaboration with cross-functional teams to advance next-generation point-of-care diagnostics from concept through commercialization. Responsibilities • Develop, optimize, and troubleshoot biochemical and clinical chemistry assays for point-of-care in vitro diagnostic platforms., • Support assay development on Lab-on-Spin-Disk, Lab-on-Disk, centrifugal microfluidic, or equivalent cartridge/analyzer-based systems., • Design and optimize reagent formulations, including enzyme systems, buffers, calibrators, stabilizers, surfactants, preservatives, and dry reagent formats., • Develop or improve lyophilized reagent bead formulations that are suitable for integration into products and transfer to manufacturing., • Evaluate assay performance parameters such as precision, accuracy, linearity, sensitivity, specificity, reportable range, interference, and matrix effects., • Conduct method comparison studies against reference analyzers or established clinical chemistry systems to demonstrate equivalence or superiority., • Support real-time and accelerated stability studies for liquid, dried, and lyophilized reagent formats., • Troubleshoot assay performance issues related to reagent chemistry, sample matrix, disk or cartridge design, fluidics, optical detection, and instrument behavior., • Work closely with engineering, instrumentation, software, manufacturing, quality assurance, quality control, and regulatory teams to ensure assay and platform compatibility., • Provide senior-level technical guidance to accelerate assay development from feasibility through product-ready design., • Support the transfer of assays from research and development into manufacturing and quality control processes., • Contribute to the development of multi-analyte clinical chemistry panels, including glucose, albumin, creatinine, lipid panels, metabolic panels, electrolyte panels, and liver function markers such as AST and ALT., • Apply statistical tools and structured experimental design to evaluate assay performance, interpret data, and drive optimization decisions., • Document development activities, protocols, and results in a clear and compliant manner to support design transfer and potential regulatory submissions.Essential Skills, • 5+ years of hands-on in vitro diagnostic assay development experience, preferably in point-of-care diagnostics, clinical chemistry, or analyzer-based systems., • Proven track record taking assays beyond feasibility into product-ready or manufacturable point-of-care IVD formats, not limited to academic research., • Hands-on experience with Lab-on-Spin-Disk, centrifugal microfluidic IVD chemistry diagnostic platforms, or closely related cartridge/analyzer-based systems., • Strong background in clinical chemistry and biochemistry assay development, particularly enzymatic and colorimetric/spectrophotometric assays for analytes such as glucose, albumin, creatinine, BUN, AST, ALT, ALP, sodium, potassium, triglycerides, and cholesterol., • Solid understanding of protein, enzyme, and antibody structure, function, and interactions as they relate to assay performance and stability., • Hands-on experience developing lyophilized reagent beads or dry/stabilized reagent formats, including formulation, optimization, stability assessment, troubleshooting, and progression toward manufacturing., • Strong experience developing assays for automated analyzers, cartridge-based systems, Lab-on-Disk platforms, or similar diagnostic platforms., • Deep knowledge of enzymatic and colorimetric/spectrophotometric assays, clinical chemistry principles, and reagent formulation strategies., • Experience translating assays from feasibility into robust product-ready designs suitable for manufacturing and commercialization., • Experience with assay verification, validation, performance characterization, and systematic troubleshooting., • Demonstrated ability to identify root causes of assay failure and implement solutions to improve robustness and reliability., • Ability to work independently as a senior technical consultant while effectively collaborating with cross-functional teams.Additional Skills & Qualifications, • PhD in Biochemistry, Analytical Chemistry, Clinical Chemistry, Chemistry, Biomedical Engineering, or a related field; or MS/BS with significant relevant industry experience., • Direct experience with Lab-on-Spin-Disk, Lab-on-Disk, centrifugal microfluidics, or similar point-of-care diagnostic platforms., • Experience developing multi-analyte clinical chemistry panels for point-of-care or analyzer-based systems., • Experience with dry chemistry, lyophilized reagent beads, reagent stabilization, or dry reagent manufacturing for IVD applications., • Experience with clinical chemistry panels such as glucose, albumin, creatinine, lipid panels, metabolic panels, electrolyte panels, liver panels, AST, ALT, and related assays., • Experience with product commercialization, design transfer, or regulatory submissions for IVD products., • Familiarity with statistical tools for assay evaluation, including regression analysis, correlation studies, Bland–Altman analysis, precision studies, and method comparison approaches., • Familiarity with GMP principles and quality systems as they apply to bioassay and IVD development., • Prior experience in diagnostics organizations developing analyzer-based or cartridge-based clinical chemistry systems is beneficial.Work Environment The role operates within a mixed office, laboratory, and manufacturing production environment in a controlled facility. Work includes time in a standard office setting for data analysis, documentation, and cross-functional collaboration, as well as extensive work in laboratory and production areas. The laboratory and production facilities are controlled clean environments that require appropriate training and adherence to safety and quality procedures. Team members may encounter potentially hazardous materials and equipment, including chemical reagents, donor blood, and automated assembly equipment. In these environments, appropriate gowning and safety practices apply, including the use of lab coats, safety glasses, gloves, and other protective equipment as required for specific activities and procedures. The organization follows equal opportunity principles and provides reasonable accommodations to enable individuals with disabilities to perform the essential functions of the role. Job Type & Location This is a Contract position based out of Monmouth Junction, NJ. Pay and Benefits The pay range for this position is $50.00 - $60.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision, • Critical Illness, Accident, and Hospital, • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available, • Life Insurance (Voluntary Life & AD&D for the employee and dependents), • Short and long-term disability, • Health Spending Account (HSA), • Transportation benefits, • Employee Assistance Program, • Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a hybrid position in Monmouth Junction,NJ. Application Deadline This position is anticipated to close on Jun 19, 2026. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options. San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records. Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability. Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.

Job DescriptionAbout GenScriptGenScript Biotech Corporation (Stock Code: 1548.HK) is a global biotechnology group. Founded in 2002, GenScript has an established global presence across North America, Europe, the Greater China, and Asia Pacific. GenScript's businesses encompass four major categories based on its leading gene synthesis technology, including operation as a Life Science CRO, enzyme and synthetic biology products, biologics development and manufacturing, and cell therapy.GenScript is committed to striving towards its vision of being the most reliable biotech company in the world to make humans and nature healthier through biotechnology. Job Overview The Associate Scientist (Management Trainee) – Molecular Biology, Gene Production Department position is designed for recent graduates with strong learning agility, leadership potential, and an interest in laboratory operations and team management. This role provides structured training in gene synthesis production, laboratory operations, continuous improvement, and leadership development. The successful candidate will work closely with experienced team leaders and supervisors to develop the technical and managerial skills required for future leadership positions within the organization. The estimated salary range is $60,000 - $75,000, depending on experience. Key Responsibilities Production & Laboratory Operations • Participate in daily molecular biology production activities, including gene synthesis and related laboratory processes., • Learn and follow laboratory SOPs, quality standards, and safety requirements., • Support production goals to ensure quality, productivity, and on-time delivery targets are achieved., • Assist with routine troubleshooting and process optimization activities., • Gain hands-on experience with laboratory equipment, automation platforms, and production workflows. Team Support & Coordination • Assist team leaders and supervisors in coordinating daily activities., • Support workload planning and task execution., • Participate in cross-functional communication and collaboration., • Help maintain a positive and productive team environment. Training & Development • Complete structured training programs in molecular biology production, quality systems, and laboratory operations., • Participate in cross-training opportunities across different production functions., • Develop technical expertise in gene synthesis workflows and related processes., • Learn leadership fundamentals, communication skills, and problem-solving methodologies. Continuous Improvement • Participate in Lean and Continuous Improvement initiatives., • Assist in identifying opportunities to improve efficiency, quality, and operational performance., • Support 5S and laboratory organization activities., • Contribute to process standardization and best-practice implementation. Problem Solving • Learn root cause analysis methodologies and structured problem-solving approaches., • Assist in investigating production issues and implementing corrective actions., • Participate in process improvement projects and performance monitoring activities. Leadership Development • Develop foundational leadership and project management skills., • Participate in mentoring and coaching programs., • Lead small improvement projects under supervision., • Build capabilities in communication, coordination, decision-making, and team collaboration., • Prepare for future advancement into Team Lead and Supervisor roles. Job Requirements Education • Master's degree in biology, Molecular Biology, Biochemistry, Biotechnology, Genetics, or a related scientific field., • Recent graduates are encouraged to apply. Experience • No prior industry experience required., • Laboratory internship, undergraduate research, capstone projects, or student leadership experience is preferred., • Exposure to molecular biology techniques is a plus. Skills • Strong learning ability and willingness to develop new skills., • Good analytical and problem-solving abilities., • Effective communication and interpersonal skills., • Ability to work independently as well as within a team environment., • Proficiency in Microsoft Office applications., • Ability to manage multiple priorities in a fast-paced environment. Competencies • Strong sense of ownership and accountability., • Positive attitude and growth mindset., • Adaptability and willingness to learn., • Team-oriented approach., • Results-driven mindset., • Demonstrated leadership potential. Other Requirements • Bachelor's degree in Life Sciences with relevant work experience will also be considered., • Prior experience in molecular cloning techniques (e.g., plasmid construction, restriction digestion, ligation, PCR, transformation) is highly preferred., • Hands-on experience in a laboratory or production setting is a plus., • Fluency in Mandarin Chinese is preferred., • Fast learner with the ability to quickly adapt to new techniques and protocols., • Must be able to work on-site in Piscataway, NJ. #LI-EB1 #GS GenScript USA Inc/ProBio Inc. is a proud equal opportunity/affirmative action employer committed to attracting, retaining, and maximizing the performance of a diverse and inclusive workforce. It is the Company's policy to ensure equal employment opportunity without discrimination or harassment based on race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity or expression, age, disability, national origin, marital or domestic/civil partnership status, genetic information, citizenship status, uniformed service member or veteran status, or any other characteristic protected by law. GenScript USA Inc./ProBio Inc. maintains a drug-free workplace. Please note: Genscript USA Inc./ProBio Inc. will only contact candidates through verified application sources. GenScript/Probio does not request personal information from candidates through individual email or any other platform.

Job DescriptionAbout GenScriptGenScript Biotech Corporation (Stock Code: 1548.HK) is a global biotechnology group. Founded in 2002, GenScript has an established global presence across North America, Europe, the Greater China, and Asia Pacific. GenScript's businesses encompass four major categories based on its leading gene synthesis technology, including operation as a Life Science CRO, enzyme and synthetic biology products, biologics development and manufacturing, and cell therapy.GenScript is committed to striving towards its vision of being the most reliable biotech company in the world to make humans and nature healthier through biotechnology.Job Overview The Plasmid Maxiprep Associate Scientist is a key role within the Plasmid Production organization, responsible for supporting daily production operations, order management, team coordination, and continuous improvement activities. This position is designed for individuals with strong technical aptitude, leadership potential, and a desire to develop into future supervisory roles. Experienced production professional or high-potential candidate with strong learning agility and scientific background are encouraged to apply. Working closely with Supervisors and Managers, the successful candidate will participate in plasmid Maxiprep production operations, production planning, cross-functional coordination, quality system execution, and team development, while supporting efficient, high-quality, and on-time delivery of customer orders. The estimated salary range is $60,000 - $75,000, depending on experience. Key ResponsibilitiesProduction Operations • Support daily plasmid Maxiprep production activities, including transformation, clone selection, culture expansion, harvesting, plasmid extraction, purification, endotoxin reduction, and product delivery., • Ensure all production activities comply with SOPs, quality standards, safety requirements, and company policies., • Monitor production schedules and order progress to ensure timely delivery of customer orders., • Assist in troubleshooting production issues and implementing effective corrective actions., • Support equipment operation, maintenance coordination, and production readiness., • Contribute to production efficiency, quality improvement, and turnaround time optimization.Order Management & Cross-Functional Coordination, • Track order progress throughout the production process and identify potential risks to delivery timelines., • Coordinate with QC, Logistics, Supply Chain, Customer Service, and other functions to ensure smooth order execution., • Support production scheduling, prioritization, and resource allocation., • Communicate production status updates and escalation items to management in a timely manner., • Participate in cross-functional discussions to support operational decision-making.Team Support & Leadership Development, • Support Supervisors in daily team coordination and workforce management., • Assist with task assignment, workload balancing, and operational support., • Provide technical guidance and on-the-job support to team members., • Participate in onboarding and training of new employees., • Support development of standardized work practices and training materials., • Foster a collaborative, accountable, and high-performance team environment., • Act as team support lead when required or during Supervisor absence.Continuous Improvement & Quality, • Participate in Lean Manufacturing and Continuous Improvement initiatives., • Identify opportunities to improve efficiency, quality, throughput, and operational performance., • Support 5S implementation, visual management, and standard work practices., • Assist in SOP updates, process optimization, and standardization activities., • Utilize Root Cause Analysis (RCA) to investigate production issues., • Support deviation investigations and CAPA implementation.QualificationsEducation, • Master's Degree in Biology, Molecular Biology, Biotechnology, Biochemistry, Genetics, or a related scientific discipline., • Demonstrated interest in laboratory operations, production management, and leadership development., • Advanced degrees are a plus.Experience, • Experience in molecular biology, biotechnology manufacturing, biopharmaceutical production, or related laboratory operations is preferred., • Experience with plasmid Maxiprep production, fermentation, purification, or related processes is preferred., • Experience in employee training, project coordination, or team support is preferred., • Supervisory or production management experience is a plus., • Candidates with strong learning agility, leadership potential, and scientific background are encouraged to apply.Skills, • Strong understanding of plasmid production processes and laboratory operations., • Hands-on experience in plasmid extraction, purification, or related workflows is preferred., • Strong analytical, troubleshooting, and problem-solving skills., • Excellent communication, interpersonal, and coordination skills., • Ability to manage multiple priorities in a fast-paced production environment., • Proficiency in Microsoft Office and production documentation systems., • Ability to analyze production data and support operational decision-making., • Bilingual proficiency in English and Mandarin Chinese (written and verbal). This role involves frequent communication with China-based teams regarding production planning, technical discussions, order coordination, issue resolution, and process optimization. Effective bilingual communication is essential to ensure accurate information flow and efficient cross-regional collaboration.Competencies, • Strong sense of ownership and accountability., • Results-driven mindset with strong execution ability., • Leadership potential and team development mindset., • Continuous improvement and operational excellence mindset., • Strong communication and collaboration skills., • Adaptability and ability to perform in a fast-paced environment., • Ability to work effectively across cross-functional and cross-regional teams.Preferred Qualifications, • Experience in plasmid Maxiprep production and manufacturing operations., • Knowledge of fermentation, harvesting, plasmid purification, and endotoxin reduction processes., • Experience in production planning, capacity management, and order scheduling., • Experience working in global or cross-regional teams, particularly U.S.–China collaboration., • Exposure to Lean Manufacturing, Continuous Improvement, or Operational Excellence initiatives., • Interest in developing into future supervisory or management roles., • Fluency in Mandarin Chinese is preferred., • Fast learner with the ability to quickly adapt to new techniques and protocols., • Must be able to work on-site in Piscataway, NJ. #LI-EB1 #GS GenScript USA Inc/ProBio Inc. is a proud equal opportunity/affirmative action employer committed to attracting, retaining, and maximizing the performance of a diverse and inclusive workforce. It is the Company's policy to ensure equal employment opportunity without discrimination or harassment based on race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity or expression, age, disability, national origin, marital or domestic/civil partnership status, genetic information, citizenship status, uniformed service member or veteran status, or any other characteristic protected by law. GenScript USA Inc./ProBio Inc. maintains a drug-free workplace. Please note: Genscript USA Inc./ProBio Inc. will only contact candidates through verified application sources. GenScript/Probio does not request personal information from candidates through individual email or any other platform.

Senior Principal Scientist – Spectroscopy (Hybrid). Location: Piscataway, New Jersey. Travel: up to 10% of time. Responsibilities Design and validate analytical protocols for active and critical inactive ingredients, stabilizers, and sensory molecules using high‑resolution LC/GC MS and NMR technologies. Lead crisis chemistry & forensic analysis, monitoring trace contaminants and root‑cause analysis on stability failures or manufacturing deviations. Conduct competitive product teardowns, use non‑targeted analysis to identify unknown components, and evaluate ingredients from new suppliers. Partner with Marketing and Legal to convert analytical results into visual science for claim validation, ensuring compliance with AOAC, USP, or ISO standards. Drive Lab 4.0 digital transformation: evaluate high‑throughput tools, implement MS imaging platforms, and build automated data pipelines for predictive machine‑learning models. Develop standardized methods for ultra‑trace extractables and leachables screening to study interactions with new sustainable or recycled packaging materials. Required Qualifications PhD in analytical, organic, or medicinal chemistry. 10 years of advanced laboratory experience. Expert knowledge of high‑resolution LC‑MS and GC‑MS for quantification and structural elucidation. Technical proficiency in FTIR, Raman, and NMR. Experience in a GxP (GLP/GMP) regulated environment with chain‑of‑custody protocols. Preferred Qualifications Experience in microbiome analytics, including metabolomics of bacterial metabolites. Background in green chemistry analytics, e.g., biodegradability of surfactants or purity of post‑consumer recycled packaging. Ability to translate complex analytical big data into actionable business strategies. Support IP activities and patent filings with detailed molecular characterization. Compensation and Benefits Salary: $124,000–$180,000 USD. Salary may include discretionary bonuses, profit‑sharing, and long‑term incentives. Benefits include medical, dental, vision, life insurance, paid parental leave, disability coverage, 401(k) plan with company match, 15 vacation/PTO days, 13 paid holidays, and paid sick leave. Equal Opportunity Employer Colgate is an equal‑opportunity employer. All qualified applicants will receive consideration without regard to race, color, religion, gender, gender identity, sexual orientation, national origin, ethnicity, age, disability, marital status, veteran status, or any other characteristic protected by law. Reasonable accommodations are available for persons with disabilities. #J-18808-Ljbffr

Medical Laboratory Scientist I - Edison, NJ - Monday-Friday 2:00pm to 10:30pm (Rotational Weekends) Quest Diagnostics is hiring a Medical Laboratory Scientist I in Edison, NJ. Medical Laboratory Scientist I- Microbiology job at Quest Diagnostics. Qualifications Qualifications: Education: BS in Medic

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The position includes structured training in laboratory operations with hands-on experience in molecular biology, aiming to prepare candidates for future managerial roles within the company. GenScript/ProBio in Piscataway, NJ, seeks a Molecular Biology Production Associate Scientist to assist in gen

Quest Diagnostics is seeking a Medical Laboratory Scientist II for its Edison, NJ location.This hospital-based role requires working every other Saturday and Sunday, and one weekday afternoon.The position offers a pay range of $32.The ideal candidate will have at least one year of experience in high

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Medical Laboratory Scientist I - Edison, NJ - Monday-Friday 2:00pm to 10:30pm (Rotational Weekends) Quest Diagnostics is hiring a Medical Laboratory Scientist I in Edison, NJ. Medical Laboratory Scientist I- Microbiology job at Quest Diagnostics. Qualifications Qualifications: Education: BS in Medic

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Job Overview The Associate Scientist (Management Trainee) – Molecular Biology, Gene Production Department position is designed for recent graduates with strong learning agility, leadership potential, and an interest in laboratory operations and team management. Key Responsibilities Production & La

Medical Laboratory Scientist based in Edison, NJ.

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Quest Diagnostics is looking for a Medical Laboratory Scientist II in Perth Amboy, NJ. Applicants should have at least one year of relevant experience and a degree in Laboratory Science or Medical Technology. Strong communication and interpersonal skills are necessary, along with proficiency in Micr

Medical Laboratory Scientist II – Perth Amboy, NJ Alternating weekly schedule: 16 hours one week, 24 hours the next. Quest Diagnostics is hiring a Medical Laboratory Scientist II in Perth Amboy, NJ. Actively support and comply with laboratory policies and procedures for specimen handling and proce

We're currently looking for individuals across the country to take part in remote paid market research, including online focus groups, product trials, and consumer studies.Earn up to $750 a week in your free time by providing feedback on everyday products and services.If you're comfortable sharing y

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Responsibilities Cleaning and organizing the Laboratory Glassware. Providing the laboratory requirements such as paper towels on each Aisle, replacing empty glove boxes, clean and dry glassware etc. Procurement of chemicals and other laboratory resources in ERP as and when required.

Job: Laboratory Technician in Analytical Lab Location: Parlin, NJ Qualifications B. Must demonstrate a history of safe laboratory practices. Experience writing laboratory test methods preferred.

We're currently looking for individuals across the country to take part in remote paid research, including remote focus groups, product trials, and consumer studies.Earn up to $750 a week in your free time by providing feedback on everyday products and services.If you're comfortable sharing your opi

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Laboratory Technician 2 - Newark, DE, 19702 Laboratory Technician - Newark, DE, 19702 New York, NY $50,000. Laboratory Technician 3 - Newark, DE, 19702 Laboratory Technician 3 (Tuesday --Saturday) _ Newark, DE, 19702 Lab Technician (Consumer Goods) - 156238 New York, NY $46,731. Responsible for perf

Murrin Murrin Operations has an opportunity for an experienced Shift Laboratory Technician to join our established and dedicated team. You will also have: Tertiary qualifications in Analytical Chemistry (TAFE Certificate, diploma or university degree) Significant experience working within an analy

Job Title Laboratory Technician I, Sanger, 6:30 pm - 3am EST Position Details Position Title: Laboratory Technician I, Sanger Location: South Plainfield, NJ Shift: M-F 6:30PM - 3AM EST Company Overview At GENEWIZ by Azenta, new ideas, new technologies and new ways of thinking are driving our fu

Ability to organize and maintain general laboratory functions, maintain accurate records, and follow laboratory safety guidelines and institutional policies. Job Title Principal Laboratory Technician (2 Vacancies) – Pediatric Hematology/Oncology – Rutgers Cancer Institute Location Downtown New

Psychiatrist's Office Office Assistant.A psychiatrist's office is seeking a part-time or full-time office assistant.The ideal candidate would have great organizational skills with the ability to multi-task and be efficient.She/he must have excellent customer service skills and be friendly.Scheduling

Edison, NJ is hiring an Entry Level Lab Technician for a full-time position, from Wednesday to Sunday, with a compensation of $17.You will perform routine lab tasks, chemical analysis, and ensure compliance with safety standards while progressing training on complex instrumentation.The ideal candida

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